gene

SLC1A2

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about SLC1A2: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

153Connections
0Hypotheses
1Analyses
50Outgoing
50Incoming
0Experiments
1Debates

Summary

SLC1A2 (EAAT2) is the primary glutamate transporter in the brain, responsible for clearing glutamate from the synaptic cleft. Dysfunction of SLC1A2 is strongly implicated in Alzheimer's disease, Parkinson's disease, and amyotrophic lateral sclerosis throu

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🧬 Gene Info
Gene SymbolSLC1A2
Full NameSolute Carrier Family 1 Member 2 (EAAT2)
AliasesEAAT2
Chromosome11p13
Protein TypeGene
Functionencodes a protein of 574 amino acids with a molecular weight of approximately 66 kDa.
Primary Expressionastrocytes surrounding synapses, where it plays a critical role in synaptic homeostasis and neuroprotection
Molecular Weight66 kDa
Amino Acids574 aa
Exons19
PathwaysTdp-43, oxidative stress response, synaptic plasticity, unfolded protein response
GeneCardsSLC1A2
Human Protein AtlasSLC1A2
AstrocytesThe primary cellular expression site, particularly perisynaptic astrocyte processes
Cerebral cortexHigh expression in layers II-IV
Associated DiseasesADHD, ALS, Alzheimer, Alzheimer's disease, anxiety
InteractionsAND, ANXIETY, APOE, App, AQP4, ASTROCYTE
KG Connections153 knowledge graph edges
DatabasesGeneCardsUniProtNCBI GeneHPASTRING

Wiki Pages (2)

Knowledge base pages for this entity

Canonical Page

SLC1A2 — Solute Carrier Family 1 Member 2 (EAAT2)

gene · 1148 words

SLC1A2 Protein — EAAT2/GLT-1

protein · 644 words

Pathway Diagram

graph TD
    SLC1A2["SLC1A2"]
    Dementia{"Dementia"}
    SLC1A2 -->|"activates"| Dementia
    Frontotemporal_Dementia{"Frontotemporal Dementia"}
    SLC1A2 -->|"activates"| Frontotemporal_Dementia
    Neurodegeneration{"Neurodegeneration"}
    SLC1A2 -->|"activates"| Neurodegeneration
    NEURODEGENERATION["NEURODEGENERATION"]
    SLC1A2 -->|"activates"| NEURODEGENERATION
    ASTROCYTES["ASTROCYTES"]
    SLC1A2 -->|"activates"| ASTROCYTES
    GJA1["GJA1"]
    GJA1 -->|"activates"| SLC1A2
    PROGRANULIN["PROGRANULIN"]
    PROGRANULIN -->|"activates"| SLC1A2
    FTLD["FTLD"]
    FTLD -->|"activates"| SLC1A2
    AQP4["AQP4"]
    AQP4 -->|"activates"| SLC1A2
    DEMENTIA["DEMENTIA"]
    DEMENTIA -->|"activates"| SLC1A2
    GRN["GRN"]
    GRN -->|"activates"| SLC1A2
    AND["AND"]
    AND -->|"activates"| SLC1A2
    NEURON["NEURON"]
    NEURON -->|"activates"| SLC1A2
    APOE["APOE"]
    APOE -->|"activates"| SLC1A2
    ASTROCYTE["ASTROCYTE"]
    ASTROCYTE -->|"activates"| SLC1A2

Outgoing (80)

TargetRelationTypeStr
ASTROCYTESexpressed_incell_type0.95
ALZHEIMER'S DISEASEassociated_withdisease0.90
PARKINSON'S DISEASEassociated_withdisease0.90
Signal Transmissioninvolved_inprocess0.90
Synaptic Degenerationsuppressesphenotype0.85

Incoming (73)

SourceRelationTypeStr
YY1downregulatesgene0.95
h-019c56c1targetshypothesis0.90
ALKBH5regulatesprotein0.90
GFAPmarkersgene0.70
RNAimplicated_ingene0.60

Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
No targeting hypotheses

Mentioning Analyses (1)

Scientific analyses that reference this entity

SEA-AD Gene Expression Profiling — Allen Brain Cell Atlas

neurodegeneration | 2026-04-02 | 5 hypotheses Top: 0.761

Experiments (0)

Experimental studies targeting or related to this entity

ExperimentTypeDiseaseScoreFeasibilityModelStatusEst. Cost
No experiments found

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found

Debates (1)

Multi-agent debates referencing this entity

Cell-type specific expression patterns of neurodegeneration genes in SEA-AD

closed · Rounds: 3 · Score: 0.68 · 2026-04-02

Related Research

Hypotheses and analyses mentioning SLC1A2 in their description or question text

No additional research found